Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Malay B Mukherjee

Showing results (1-10 of 41) with videos related to

Pageof 5
Sort By:
Current Opinion in Hematology|February 15, 2002
Sickle cell disease in IndiaDipika Mohanty, Malay B Mukherjee
Indian Journal of Human Genetics|July 4, 2012
Explaining anthropometric variations in sickle cell disease requires a multidimensional approachMalay B Mukherjee, Kanjaksha Ghosh
The Indian Journal of Medical Research|July 4, 2015
Haemoglobinopathies in tribal populations of IndiaKanjaksha Ghosh, Roshan B Colah, Malay B Mukherjee
International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Sickle Cell Disease: Indian ExperienceRoshan B Colah, Pallavi Mehta, Malay B Mukherjee
Indian Journal of Pediatrics|July 1, 2004
Glucose-6-phosphate dehydrogenase deficiency in IndiaDipika Mohanty, Malay B Mukherjee, Roshan B Colah
The Indian Journal of Medical Research|July 4, 2015
Sickle cell disease in tribal populations in IndiaRoshan B Colah, Malay B Mukherjee, Snehal Martin, et al.
Blood Cells, Molecules & Diseases|July 6, 2005
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutationSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
International Journal of Laboratory Hematology|March 20, 2024
Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A reviewPallavi Thaker, Namrata Mahajan, Malay B Mukherjee, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 30, 2011
G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in IndiaSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Molecular basis of G6PD deficiency in IndiaSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Current Opinion in Hematology|February 15, 2002
Sickle cell disease in IndiaDipika Mohanty, Malay B Mukherjee
Indian Journal of Human Genetics|July 4, 2012
Explaining anthropometric variations in sickle cell disease requires a multidimensional approachMalay B Mukherjee, Kanjaksha Ghosh
The Indian Journal of Medical Research|July 4, 2015
Haemoglobinopathies in tribal populations of IndiaKanjaksha Ghosh, Roshan B Colah, Malay B Mukherjee
International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Sickle Cell Disease: Indian ExperienceRoshan B Colah, Pallavi Mehta, Malay B Mukherjee
Indian Journal of Pediatrics|July 1, 2004
Glucose-6-phosphate dehydrogenase deficiency in IndiaDipika Mohanty, Malay B Mukherjee, Roshan B Colah
The Indian Journal of Medical Research|July 4, 2015
Sickle cell disease in tribal populations in IndiaRoshan B Colah, Malay B Mukherjee, Snehal Martin, et al.
Blood Cells, Molecules & Diseases|July 6, 2005
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutationSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
International Journal of Laboratory Hematology|March 20, 2024
Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A reviewPallavi Thaker, Namrata Mahajan, Malay B Mukherjee, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 30, 2011
G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in IndiaSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Molecular basis of G6PD deficiency in IndiaSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
Pageof 5